Abstract

Context:Maternal obesity and gestational diabetes mellitus (GDM) can both contribute to adverse neonatal outcomes. The extent to which this may be mediated by differences in placental metabolism and nutrient transport remains to be determined.Objective:Our objective was to examine whether raised maternal body mass index (BMI) and/or GDM contributed to a resetting of the expression of genes within the placenta that are involved in energy sensing, oxidative stress, inflammation, and metabolic pathways.Methods:Pregnant women from Spain were recruited as part of the “Study of Maternal Nutrition and Genetics on the Foetal Adiposity Programming” survey at the first antenatal visit (12–20 weeks of gestation) and stratified according to prepregnancy BMI and the incidence of GDM. At delivery, placenta and cord blood were sampled and newborn anthropometry measured.Results:Obese women with GDM had higher estimated fetal weight at 34 gestational weeks and a greater risk of preterm deliveries and cesarean section. Birth weight was unaffected by BMI or GDM; however, women who were obese with normal glucose tolerance had increased placental weight and higher plasma glucose and leptin at term. Gene expression for markers of placental energy sensing and oxidative stress, were primarily affected by maternal obesity as mTOR was reduced, whereas SIRT-1 and UCP2 were both upregulated. In placenta from obese women with GDM, gene expression for AMPK was also reduced, whereas the downstream regulator of mTOR, p70S6KB1 was raised.Conclusions:Placental gene expression is sensitive to both maternal obesity and GDM which both impact on energy sensing and could modulate the effect of either raised maternal BMI or GDM on birth weight.

Highlights

  • Context: Maternal obesity and gestational diabetes mellitus (GDM) can both contribute to adverse neonatal outcomes

  • Birth weight was unaffected by body mass index (BMI) or GDM; women who were obese with normal glucose tolerance had increased placental weight and higher plasma glucose and leptin at term

  • Placental gene expression is sensitive to both maternal obesity and GDM which both impact on energy sensing and could modulate the effect of either raised maternal BMI or GDM on birth weight. (J Clin Endocrinol Metab 101: 59 – 68, 2016)

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Summary

Methods

Pregnant women from Spain were recruited as part of the “Study of Maternal Nutrition and Genetics on the Foetal Adiposity Programming” survey at the first antenatal visit (12–20 weeks of gestation) and stratified according to prepregnancy BMI and the incidence of GDM. Participants The subjects participated in a Spanish longitudinal study on the influence of body composition by maternal genetics and nutrition (“Study of Maternal Nutrition and Genetics on the Foetal Adiposity Programming” [PREOBE] study: P06-CTS02341) undertaken between 2007 and 2010 and registered with www.ClinicalTrials.gov, (NCT01634464) [31, 32]. In the overall PREOBE study (Figure 1), 474 pregnant women aged 18 – 45, with singleton pregnancies, were assessed for eligibility between 12–20 weeks’ gestation at two different primary health care settings (Clinical University Hospital “San Cecilio” and the “Mother-Infant” University Hospital) in Granada, Spain. 79 women were diagnosed with GDM following measurement of raised fasting plasma glucose concentrations, 25 women after a 75-g oral glucose tolerance test between 16 and 18 weeks’ gestation [11], if they either had a family history of GDM or had previously had GDM, or were obese, whereas 54 women were diagnosed after an additional 100-g oral glucose tolerance test between 24 and 28 weeks’ gestation

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